Guazzarotti L - Search Results

1

Vomer aplasia in a patient carrying a de novo mutation of the TP63 gene (3q27).

Schindler A, Guazzarotti L, Mameli C, Urbani E, Mozzanica F, Guerrini L, Zuccotti GV. Schindler A, et al. Among authors: guazzarotti l. Int J Pediatr Otorhinolaryngol. 2013 Sep;77(9):1606-8. doi: 10.1016/j.ijporl.2013.06.027. Epub 2013 Jul 29. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23906991 Review.

2

Limb-mammary syndrome (LMS) associated with internal female genitalia dysgenesia: a new genotype/phenotype correlation?

Guazzarotti L, Caprio C, Rinne TK, Bosoni M, Pattarino G, Mauri S, Tadini GL, van Bokhoven H, Zuccotti GV. Guazzarotti L, et al. Am J Med Genet A. 2008 Aug 1;146A(15):2001-4. doi: 10.1002/ajmg.a.32371. Am J Med Genet A. 2008. PMID: 18627043 No abstract available.

3

T lymphocyte maturation is impaired in healthy young individuals carrying trisomy 21 (Down syndrome).

Guazzarotti L, Trabattoni D, Castelletti E, Boldrighini B, Piacentini L, Duca P, Beretta S, Pacei M, Caprio C, Vigan Ago A, di Natale B, Zuccotti GV, Clerici M. Guazzarotti L, et al. Am J Intellect Dev Disabil. 2009 Mar;114(2):100-9. doi: 10.1352/2009.114.100-109. Am J Intellect Dev Disabil. 2009. PMID: 19391670

4

Immunomodulating activity of Pidotimod in children with Down syndrome.

Zuccotti GV, Mameli C, Trabattoni D, Beretta S, Biasin M, Guazzarotti L, Clerici M. Zuccotti GV, et al. Among authors: guazzarotti l. J Biol Regul Homeost Agents. 2013 Jan-Mar;27(1):253-8. J Biol Regul Homeost Agents. 2013. PMID: 23489705 Clinical Trial.

5

Phenotypic heterogeneity and mutational spectrum in a cohort of 45 Italian males subjects with X-linked ectodermal dysplasia.

Guazzarotti L, Tadini G, Mancini GE, Giglio S, Willoughby CE, Callea M, Sani I, Nannini P, Mameli C, Tenconi AA, Mauri S, Bottero A, Caimi A, Morelli M, Zuccotti GV. Guazzarotti L, et al. Clin Genet. 2015 Apr;87(4):338-42. doi: 10.1111/cge.12404. Epub 2014 May 30. Clin Genet. 2015. PMID: 24724966

6

WNT10A gene is the second molecular candidate in a cohort of young Italian subjects with ectodermal derivative impairment (EDI).

Guazzarotti L, Tadini G, Mancini GE, Sani I, Pisanelli S, Galderisi F, D'Auria E, Secondi R, Bottero A, Zuccotti GV. Guazzarotti L, et al. Clin Genet. 2018 Mar;93(3):693-698. doi: 10.1111/cge.13147. Epub 2017 Nov 8. Clin Genet. 2018. PMID: 28976000

7

Mechanisms and management of growth impairment in children affected by inflammatory bowel disease.

Dilillo D, Guazzarotti L, Galli E, Zuccotti GV. Dilillo D, et al. Among authors: guazzarotti l. Expert Rev Endocrinol Metab. 2013 May;8(3):289-299. doi: 10.1586/eem.13.12. Expert Rev Endocrinol Metab. 2013. PMID: 30780818

8

First Year Metabolic and Hormonal Behavior Define two Different Populations of SGA Newborn for Weight or Height.

Guazzarotti L, Mauri S, Santi D, Pogliani L, Zuccotti G. Guazzarotti L, et al. J Endocr Soc. 2022 Feb 21;6(5):bvac028. doi: 10.1210/jendso/bvac028. eCollection 2022 May 1. J Endocr Soc. 2022. PMID: 35350393 Free PMC article.

9

Appropriate management of growth hormone deficiency during the age of transition: an Italian Delphi consensus statement.

Cannavò S, Cappa M, Ferone D, Isidori AM, Loche S, Salerno M, Maghnie M; Delphi panel members (paediatric, adult endocrinologists). Cannavò S, et al. J Endocrinol Invest. 2023 Jan;46(1):189-200. doi: 10.1007/s40618-022-01880-w. Epub 2022 Aug 12. J Endocrinol Invest. 2023. PMID: 35960476 Free article. No abstract available.

10

Efficacy and safety of growth hormone treatment in children with short stature: the Italian cohort of the GeNeSIS clinical study.

Cappa M, Iughetti L, Loche S, Maghnie M, Vottero A; GeNeSIS National Board on behalf of the GeNeSIS Italian Investigators. Cappa M, et al. J Endocrinol Invest. 2016 Jun;39(6):667-77. doi: 10.1007/s40618-015-0418-0. Epub 2015 Dec 28. J Endocrinol Invest. 2016. PMID: 27223400 Free PMC article.

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